Medical devices protect the health of people by supporting the medical sciences from research and development to diagnosis, treatment and care. Terasaki has obtained ISO13485 certification for the quality assurance program we have put in place for the medical devices we produce. We are meeting the needs of customers with a complete system of development, design and manufacture based on the know-how we have accumulated with electrics, electronics and control over the decades since our founding.
Terasaki realizes optimized designs through 3D CAD, software development, real time OS, efficient system design, suitable PCB, mould and sheet metal designs and proper structural design, resin flow analysis and more.
Before finalizing products for mass-production, Terasaki goes through a series of prototypes in order to tangibly shape customer requirements, and maximize cost-performance in ways that ensure efficient manufacture.
Terasaki tests products against temperature, humidity and other environmental conditions, as well as EMC and electrical safety requirements. Results are then fed back to development to improve quality.
Terasaki has a variety of tools and technologies at its disposition to engineer manufacturing for both mass-production and flexible lot-based production. In fact, it is considered one of our specialties to build systems to ensure planned results and shorten development cycles by intelligently integrating development and manufacturing.
Engineers are always on hand at Terasaki to provide field support to products in the marketplace.
Terasaki assures product quality via a well-rounded system of detailed troubleshooting and corrective measures, preventative measures, periodic audits of suppliers and regular quality discussions with customers.
Terasaki fully understands that maintaining the confidentiality of medical device manufacturers and research institutes is an essential requirement of this field of business.
